chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3155348130155348131TC15GENICheterozygous57746758
3155348220155348221AG17GENICheterozygous57746760
3155348417155348418AG14GENICheterozygous57746762
3155348625155348626GA14GENICheterozygous57746764
3155349066155349067AT13GENICheterozygous57746766
3155349743155349744CT17GENICheterozygous57746768
3155350573155350574C-12GENICheterozygous57746770
3155351353155351354CT15GENICheterozygous57746772
3155351443155351444TC13GENICheterozygous57746774
3155351502155351503TC12GENICheterozygous57746776
3155351710155351711AG12GENICheterozygous57746778
3155354845155354846CA16GENICheterozygous57746783
3155355388155355389CG9GENIChomozygous57746784
3155355525155355526CT13GENICheterozygous57746786
3155356892155356893AG7GENICheterozygous57746788
3155357267155357268GC10GENICheterozygous57746796
3155359006155359007CA10GENICheterozygous57746800
3155359157155359158CT19GENICheterozygous57746802
3155359213155359214TC19GENICheterozygous57746804
3155359292155359293TC18GENICheterozygous57746806
3155359633155359634CT9GENIChomozygous57746807
3155359678155359679CT9GENIChomozygous57746809
3155362732155362733TA18GENICheterozygous57746825
3155362827155362828GT20GENICheterozygous57746827
3155362878155362879CT19GENICheterozygous57746828
3155364780155364781TC20GENICheterozygous57746832
3155369420155369421TG18GENICheterozygous57746838
3155371277155371278CT10GENICheterozygous57746841
3155371845155371846GA10GENICheterozygous57746843